HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010577Generated: October 26, 2026
Methane → N-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamide
https://huagongshe.com/reaction/1010577
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | N-(2-acetylphenyl)benzenesulfonamide | HCID 3479040 | — |
| Product | N-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamide | HCID 57429080 | 46% |
Reaction Steps
1 ml of water, 1 g activated charcoal and 2.66 g (24 mmol) selenium dioxide was added to a solution of 1.65 g (6.00 mmol) N-(acetylphenyl)benzenesulphonamide in about 10 mL dioxane. The reaction mixture was stirred for approx. 4 d at 80° C. and then the solvent was eliminated using the rotary evaporator. The residue was dissolved in about 30 ml of ethanol and refluxed for approx. 4 h. The solvent was eliminated from the reaction mixture using the rotary evaporator, the residue was dissolved in about 100 mL ethyl acetate, washed about three times with 30 ml saturated aqueous sodium hydrogen carbonate solution, dried over sodium sulphate and the solvent was eliminated using the rotary evaporator. 0.917 g (2.73 mmol, 46%) N-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamide were obtained as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07977334B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-ef6e5f3802194fe1a97537263c90f728 |
|---|
| Source note | uspto-grants-2011_07 |
|---|